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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534001Generated: October 26, 2026

Chloroiodomethane → (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone

https://huagongshe.com/reaction/534001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylateHCID 853165—
ReactantLithium diisopropylamideHCID 2724682—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanoneHCID 8664414842%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (S)-methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate (1.3 g, 8.1 mmol) and chloroiodomethane (4.3 g, 24 mmol) in THF (50 mL) at −78° C. was added a solution of LDA (16.2 mL, 24 mmol) in portions over 10 minutes. The reaction was stirred at −78° C. for 10 minutes. To this mixture was added a 10% solution of acetic acid (50 mL) in THF at −78° C. After addition, the slurry was warmed to ambient temperature. The reaction was poured into EtOAc (200 mL) and the aqueous layer basified using 1 N NaOH. The organics were separated and washed with brine, dried over MgSO4 and concentrated in vacuo. The material was purified by chromatography using DCM as eluent to give (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone (0.60 g, 3.4 mmol, 42% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-b7c4027cdc354a2db8ea9cd6545bf4b5
Source noteuspto-grants-2014_10